R&D Programmer IV
Date: March 11, 2025
Location: Bangalore, India, 560064
Company: Teva Pharmaceuticals
Job ID: 61013
Who We Are:
Teva Pharmaceuticals is a global leader in generic medicines and a proud producer of numerous products on the World Health Organization’s Essential Medicines List. With operations in nearly 60 countries and a diverse workforce, we serve millions worldwide by making healthcare more affordable and accessible. Today, at least 200 million people globally take one of our medicines daily, and we’re continuously striving to extend our positive impact by innovating and bringing in new talent.
The Opportunity:
As a Clinical Programming Manager in R&D Programming, you will be responsible for managing the timely and accurate execution of programming components in clinical trials. This role involves leading and managing completed projects that include global tasks, cross-functional teams, and outsourcing resources. You will also contribute to designing and analyzing clinical trials, including programming rules and mocked T/L/Gs. Additionally, you will provide safety claims for new drugs and support publication and extension claims for marketed drugs.
How You’ll Spend Your Day:
Budget Planning: Provide input for budget planning and resource allocation.
Vendor and Training Oversight: Likely to oversee contingent workers and vendors and provide training to others.
Project-Level Work: Primarily works at the project level, ensuring quality and timely delivery.
Strategy Contribution: Contribute to strategy development with moderate supervision.
Programming and Validation: Provide strong programming support to CDISC-based e-submission. Develop, review, and validate generic SAS macros. Develop, debug, and enhance SAS programs for quality control of safety and efficacy datasets.
Statistical Model Knowledge: Apply understanding of statistical models in efficacy data analysis.
Standardization of Deliverables: Responsible for standardizing clinical programming deliverables within a project.
Process Improvement: Extend or develop new clinical programming methods to solve complex problems.
Your Experience and Qualifications:
Education:
Bachelor’s Degree, Master’s Degree, or PhD in Science, Statistics, Information Technology, or a related field.
Experience:
Bachelor’s Degree with 5+ years of experience, or
Master’s Degree with 4+ years of experience in a pharmaceutical or clinical research setting as a programmer.
Technical Knowledge:
Experience in SDTM and ADaM, with knowledge of CDISC Guidelines and Requirements.
Proficiency in SAS Programming with expertise in clinical programming and statistical models.
Teva’s Equal Employment Opportunity Commitment:
Teva Pharmaceuticals is committed to equal opportunity in employment. We ensure that all qualified applicants are considered without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin, or any other legally protected status.
If you are contacted for a job opportunity, please inform us of any accommodations needed to facilitate an inclusive and accessible candidate experience.
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